Shafuddin Eskandarain, Mills Graham D, Holmes Mark D, Poole Phillippa J, Mullins Peter R, Black Peter N
Respiratory Research Unit, Department of Respiratory Medicine, Waikato Hospital, Hamilton, New Zealand.
Respiratory Clinical Trials Unit, Royal Adelaide Hospital, Adelaide, SA, Australia.
J Negat Results Biomed. 2015 Sep 7;14:15. doi: 10.1186/s12952-015-0034-8.
Azithromycin prophylaxis has been shown to reduce COPD exacerbations but there is poor evidence for other antibiotics. We compared exacerbation rates in COPD patients with a history of frequent exacerbations (at least three moderate or severe COPD exacerbations in the past two years) during a 12-week treatment course and over a subsequent 48-week follow up period.
292 patients were randomised to one of three treatments for 12 weeks: roxithromycin 300 mg daily and doxycycline 100 mg daily (n = 101); roxithromycin 300 mg daily (n = 97); or matching placebos (n = 94). There were no differences in the annualised moderate and severe exacerbation rates after treatment with roxithromycin/doxycycline (2.83 (95 % CI 2.37-3.40)) or roxithromycin only (2.69 (2.26-3.21)) compared to placebo (2.5 (2.08-3.03)) (p = 0.352 and p = 0.5832 respectively). Furthermore, there were no differences in the annualised exacerbation rates during 12-week treatment with roxithromycin/doxycycline (1.64 (95 % CI 1.17-2.30)), roxithromycin only (1.75 (1.24-2.41)) or placebo (2.23 (1.68-3.03)) (p = 0.1709 and p = 0.2545 respectively). There were also no significant differences between groups for spirometry or quality of life scores over either the 12-week treatment or 48-week post-treatment periods. Both active treatments were associated with nausea but otherwise adverse events were comparable among treatment groups.
Twelve-weeks of prophylaxis with roxithromycin/doxycycline combination or roxithromycin alone did not reduce COPD exacerbations in patients with history of frequent exacerbations. These findings do not support the use of these antibiotics to prevent exacerbations in COPD patients.
阿奇霉素预防已被证明可减少慢性阻塞性肺疾病(COPD)急性加重,但其他抗生素的证据不足。我们比较了有频繁急性加重病史(过去两年中至少有三次中度或重度COPD急性加重)的COPD患者在12周治疗疗程及随后48周随访期内的急性加重率。
292例患者被随机分为三种治疗方案之一,治疗12周:每日罗红霉素300mg加每日强力霉素100mg(n = 101);每日罗红霉素300mg(n = 97);或匹配的安慰剂(n = 94)。与安慰剂(2.5(2.08 - 3.03))相比,罗红霉素/强力霉素治疗后(2.83(95%CI 2.37 - 3.40))或仅用罗红霉素治疗后(2.69(2.26 - 3.21))的年化中度和重度急性加重率无差异(分别为p = 0.352和p = 0.5832)。此外,在12周治疗期间,罗红霉素/强力霉素(1.64(95%CI 1.17 - 2.30))、仅用罗红霉素(1.75(1.24 - 2.41))或安慰剂(2.23(1.68 - 3.03))的年化急性加重率无差异(分别为p = 0.1709和p = 0.2545)。在12周治疗期或治疗后48周期间,各治疗组间的肺功能测定或生活质量评分也无显著差异。两种活性治疗均与恶心相关,但除此之外,各治疗组间的不良事件相当。
罗红霉素/强力霉素联合或单用罗红霉素进行12周预防,并未降低有频繁急性加重病史的COPD患者的急性加重率。这些结果不支持使用这些抗生素预防COPD患者的急性加重。